@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP81578.RAB6_kFpNAqY_MKRAiXb27r5EZaPDdaRxO0T8-Q-a2Gts
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
np:hasAssertion
dgn-np:NP81578.RAB6_kFpNAqY_MKRAiXb27r5EZaPDdaRxO0T8-Q-a2Gts130_assertion
;
np:hasProvenance
dgn-np:NP81578.RAB6_kFpNAqY_MKRAiXb27r5EZaPDdaRxO0T8-Q-a2Gts130_provenance
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np:hasPublicationInfo
dgn-np:NP81578.RAB6_kFpNAqY_MKRAiXb27r5EZaPDdaRxO0T8-Q-a2Gts130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP81578.RAB6_kFpNAqY_MKRAiXb27r5EZaPDdaRxO0T8-Q-a2Gts130_assertion
a
np:Assertion
.
dgn-np:NP81578.RAB6_kFpNAqY_MKRAiXb27r5EZaPDdaRxO0T8-Q-a2Gts130_provenance
a
np:Provenance
.
dgn-np:NP81578.RAB6_kFpNAqY_MKRAiXb27r5EZaPDdaRxO0T8-Q-a2Gts130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP81578.RAB6_kFpNAqY_MKRAiXb27r5EZaPDdaRxO0T8-Q-a2Gts130_assertion
{
miriam-gene:6583
a
ncit:C16612
.
lld:C0021390
a
ncit:C7057
.
dgn-gda:DGN71d31b710f99cc43a8873f655285693e
sio:SIO_000628
miriam-gene:6583
,
lld:C0021390
;
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.
}
dgn-np:NP81578.RAB6_kFpNAqY_MKRAiXb27r5EZaPDdaRxO0T8-Q-a2Gts130_provenance
{
dgn-np:NP81578.RAB6_kFpNAqY_MKRAiXb27r5EZaPDdaRxO0T8-Q-a2Gts130_assertion
dcterms:description
"[Our results indicate that although OCTN or CARD15 variation is associated with susceptibility to IBD in Western populations, these might be rare and may not be associated with susceptibility to IBD in Chinese patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:18756601
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP81578.RAB6_kFpNAqY_MKRAiXb27r5EZaPDdaRxO0T8-Q-a2Gts130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:40+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
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> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
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"v2.1.0" .
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